创伤后应激障碍和酒精使用障碍预测细胞衰老的速度

Sage E. Hawn , Xiang Zhao , Mark W. Miller , Sara Wallander , Christine Govan , Anjanette Stone , Steven A. Schichman , Mark W. Logue , Erika J. Wolf
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引用次数: 0

摘要

晚期表观遗传学年龄与精神病理学有关,可能有助于解释精神病理学与身体健康发病率和死亡率之间的联系。使用171名暴露于创伤的退伍军人的纵向样本,我们使用两种表观遗传学年龄算法(GrimAge和Horvath)模拟了两个时间点(平均间隔5.58年)的表观遗传年龄变化率,并测试了与创伤后应激障碍(PTSD)、酒精使用障碍(AUD)和抑郁症的关系。结果显示,随着时间的推移,PTSD(β=0.199)和AUD(β=1.186)与表观遗传学衰老速度加快有关(ps<;.021)。结果复制和扩展了先前的工作,并为在精神病理学患者中确定减缓生物衰老速度的干预措施提供了基础支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PTSD and alcohol use disorders predict the pace of cellular aging

Advanced epigenetic age is associated with psychopathology and may help to explain the link between psychopathology and physical health morbidity and mortality. Using a longitudinal sample of 171 trauma-exposed Veterans, we modeled the rate of change in epigenetic age across two time points (averaging 5.58 years apart) using two epigenetic age algorithms (GrimAge and Horvath) and tested associations with posttraumatic stress disorder (PTSD), alcohol use disorder (AUD), and depression. Results showed that PTSD (β = .199) and AUD (β = .186) were associated with a quickened pace of epigenetic aging over time (ps <.021). Results replicate and extend prior work and offer foundational support for identifying interventions that slow the pace of biological aging among those with psychopathology.

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来源期刊
Journal of mood and anxiety disorders
Journal of mood and anxiety disorders Applied Psychology, Experimental and Cognitive Psychology, Clinical Psychology, Psychiatry and Mental Health, Psychology (General), Behavioral Neuroscience
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